Medical DeviceJun 10, 2026
CareFusion 303 BD Pyxis MedBank Tower REF: 1145-00 Medication cabinet recall — FDA Z-2303-2026
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Class IIFDA: OngoingCareFusion 303, Inc.
Recall history in this database
Classification mix: Class II: 101, Class I: 30, Class III: 1.
Medical DeviceJun 10, 2026
CareFusion 303 BD Pyxis Mini Main REF: 349 Medication cabinet recall — FDA Z-2301-2026
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Class IIFDA: OngoingCareFusion 303, Inc.
Medical DeviceJun 10, 2026
CareFusion 303 BD Pyxis Anesthesia Station 4000 REF: 338 Medication cabinet recall — FDA Z-2300-2026
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Class IIFDA: OngoingCareFusion 303, Inc.
Medical DeviceJun 10, 2026
CareFusion 303 BD Pyxis MedStation ES REF: 323 Medication cabinet recall — FDA Z-2298-2026
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Class IIFDA: OngoingCareFusion 303, Inc.
Medical DeviceJun 10, 2026
CareFusion 303 BD Pyxis Anesthesia Station ES REF: 327 Medication cabinet recall — FDA Z-2299-2026
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Class IIFDA: OngoingCareFusion 303, Inc.
Medical DeviceJun 10, 2026
CareFusion 303 BD Pyxis MedStation 4000 REF: 303 Medication cabinet recall — FDA Z-2297-2026
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Class IIFDA: OngoingCareFusion 303, Inc.
Medical DeviceJun 10, 2026
CareFusion 303 BD Pyxis MedBank Mini REF: 1147-00 Medication cabinet recall — FDA Z-2304-2026
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Class IIFDA: OngoingCareFusion 303, Inc.
Medical DeviceJun 10, 2026
CareFusion 303 BD Pyxis MedStation ES Tower REF: 352 Medication cabinet recall — FDA Z-2302-2026
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Class IIFDA: OngoingCareFusion 303, Inc.
Medical DeviceApr 1, 2026
CareFusion 303 BD Alaris" System with Guardrails" Suite MX with Point of Care Unit recall — FDA Z-1645-2026
Due to product labeling not indicating which Transport Layer Security (TLS) version that must be enabled on hospital network to ensure secure Wi-Fi communication with Point-of-Care Units
Class IIFDA: OngoingCareFusion 303, Inc.
Medical DeviceFeb 4, 2026
CareFusion 303 BD Alaris" Pump Module model 8100 UDI-DI code: 10885403810046 The BD AlarisTM recall — FDA Z-1217-2026
Due to a number of modules flashed with a date and time associated with the daylight savings time (DST) adjustment that may cause connectivity issue with hospital networks. This issue only…
Class IIFDA: OngoingCareFusion 303, Inc.
Medical DeviceJan 14, 2026
CareFusion 303 BD Pyxis ES Enterprise Server Catalog Numbers 1115-00, 137672-02,137672-03 recall — FDA Z-1028-2026
Due a software issue that may result in equipment not receiving timely updates of patient, medication, or related information from enterprise systems.
Class IIFDA: OngoingCareFusion 303, Inc.
Medical DeviceDec 31, 2025
CareFusion 303 BD Pyxis MedStation ES, REF: 323, BD Pyxis MedStation ES 7 Drawer Auxiliary recall — FDA Z-0962-2026
Automated Dispensing Cabinets (ADC) received a Half Height CUBIE drawer firmware update, which caused a Cubie Insert event which prompts software to generate a duplicate address, which…
Class IIFDA: OngoingCareFusion 303, Inc.
Medical DeviceNov 26, 2025
CareFusion 303 BD Alaris infusion Pump Module 8100, REF: 8100 recall — FDA Z-0430-2026
If infusion pump is dropped or severely jarred this may damage the pump module bezel assembly, which can cause under-infusion, over-infusion, unregulated flow, or pump module failure to…
Class IFDA: OngoingCareFusion 303, Inc.
Medical DeviceNov 5, 2025
CareFusion 303 Various models of BD Pyxis MedFlex, Reference numbers: 1119-00 1139-00 recall — FDA Z-0368-2026
Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
Class IIFDA: OngoingCareFusion 303, Inc.
Medical DeviceNov 5, 2025
CareFusion 303 Various models of BD Pyxis Pro 7-Drawer Auxiliary, Reference numbers: 1149-00 recall — FDA Z-0369-2026
Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
Class IIFDA: OngoingCareFusion 303, Inc.
Medical DeviceNov 5, 2025
CareFusion 303 All Serial Numbers/BD Pyxis CII Safe ES Tower Main, REF: 1116-00 recall — FDA Z-0371-2026
Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
Class IIFDA: OngoingCareFusion 303, Inc.
Medical DeviceNov 5, 2025
CareFusion 303 Various models of BD Pyxis Medbank: Reference numbers: 1137-00 1145-00 recall — FDA Z-0367-2026
Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
Class IIFDA: OngoingCareFusion 303, Inc.
Medical DeviceOct 15, 2025
CareFusion 303 BD Alaris Pump Infusion Sets for the following reference numbers: C24101E recall — FDA Z-0035-2026
Infusion pump module used with compatible pump infusion sets may perform outside the established performance ranges for flow rate and bolus accuracy, downstream and upstream occlusion time…
Class IFDA: OngoingCareFusion 303, Inc.
Medical DeviceSep 3, 2025
CareFusion 303 BD Pyxis Product Name / UDI-DI code / Catalog No recall — FDA Z-2477-2025
Antivirus software was not consistently installed on impacted devices during the implementation process.
Class IIFDA: OngoingCareFusion 303, Inc.
Medical DeviceAug 20, 2025
CareFusion 303 Description/REF: BD PYXIS MEDBANK MINI 1FH-1FM/169-137, BD PYXIS MEDBANK MINI recall — FDA Z-2321-2025
Reports of delayed access to medication in automated dispensing cabinets because of the override/Add Item workflow.
Class IIIFDA: OngoingCareFusion 303, Inc.
Medical DeviceAug 13, 2025
CareFusion 303 BD Alaris Pump Infusion Sets REF: 10013186, BD Alaris Pump Infusion Set, Back recall — FDA Z-2180-2025
Infusion pump module used with compatible pump infusion sets may perform outside the established performance ranges for flow rate and bolus accuracy, downstream and upstream occlusion time…
Class IFDA: OngoingCareFusion 303, Inc.
Medical DeviceAug 13, 2025
CareFusion 303 BD Alaris Pump Module Model, 8100 with Guardrails, Suite MX software versions recall — FDA Z-2179-2025
Infusion pump module used with compatible pump infusion sets may perform outside the established performance ranges for flow rate and bolus accuracy, downstream and upstream occlusion time…
Class IFDA: OngoingCareFusion 303, Inc.
Medical DeviceJul 2, 2025
CareFusion 303 Product Name [REF]: Supply Server, CCE Enterprise SW Site License (2-5), BD recall — FDA Z-2017-2025
During automated dispensing cabinet upgrade/installation/reimaging, component manager was left in installed mode, and if a Microsoft patch is then installed this may lead to an error…
Class IIFDA: OngoingCareFusion 303, Inc.
Medical DeviceApr 30, 2025
CareFusion 303 BD PYXIS MEDBANK (Name, REF): MEDPASS MODULE, 139088-01 recall — FDA Z-1639-2025
Users trying to restock a single bin location of an automated dispensing cabinet, during pocket exchange restocking workflow, may experience a software issue that results in 2 destock…
Class IIFDA: OngoingCareFusion 303, Inc.
Understanding this recall history
This page summarizes recall records in which the official source identifies CareFusion 303, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.